Siemens Careers

PT-Sr Mgr, Project Mgmt (Tech)

East Walpole, Massachusetts
Project Management

English (US)

Job Description

Division: Siemens Healthineers
Business Unit: Laboratory Diagnostics
Requisition Number: 219317
Primary Location: United States-Massachusetts-East Walpole
Assignment Category: Full-time regular
Experience Level: Senior level
Education Required Level: Bachelor's Degree
Travel Required: 20%

Division Description:

Siemens is a global technology powerhouse that has stood for engineering excellence, innovation, quality, reliability and internationality for more than 165 years. As a global technology company, Siemens is rigorously leveraging the advantages that this setup provides. To tap business opportunities in both new and established markets, the Company is organized in nine Divisions: Power and Gas, Wind Power and Renewables, Energy Management, Building Technologies, Mobility, Digital Factory, Process Industries and Drives, Healthineers and Financial Services.

 With 45,000 employees Siemens Healthineers is one of the world’s largest suppliers of technology to the healthcare industry and a leader in medical imaging, laboratory diagnostics and healthcare IT. All supported by a comprehensive portfolio of clinical consulting, training, and services available across the globe and tailored to customers’ needs. So that more people can have a life that is longer, richer, and more filled with happiness.

 For more information, please visit:

Job Description:

Position Overview
Key Management and Leadership role in Technology Transfer, supporting the manufacturing transfer of Centaur products from Walpole to Shanghai as part of project DRACO.
Key purpose of this role is to provide managerial support and technical guidance to TECTRN Project Managers as they support Wave Transfer teams and other DRACO Core team functions to facilitate resolution of complex process, compliance and project management issues associated with the Siemens Manufacturing expansion project in Shanghai.  Areas of focus include; Document preparation, BOMs, Routings and SMNs development, Scheduling and planning production builds. Other areas of support include; Test method validation, Product Performance Evaluations, Product Technical Requirements development, CFDA Clinical Trial support, CFDA submission support, Documentation development, and Design Control, both at the Walpole and Shanghai facilities.
Individual will be specifically responsible for;
  • Direct supervision and management of Project Managers.
  • Lead cross-functional element teams as needed.
  • Develop strategies, drive decisions, develop plans and implement actions that will drive on-time completion of DRACO Master and Wave schedules
  • Facilitate cross functional communication and collaboration within DRACO project to identify and eliminate roadblocks. Develop new processes as needed.
  • Support Design Control efforts including Design Change, Verification, Validation, Risk Management/Process Change, Manufacturing Transfer, with technical support and project Management support. This may include Plan and Report writing, technical evaluation of needed
  • Develop tracking tool for issues/projects/timelines
  • Ensure alignment and integration with DRACO master schedule
  • Communicate status of issues/projects  a regular basis to DRACO Core team
Desired Skills
  • Understanding of the assay architecture and design of immunoassays, manufacturing experience a plus.
  • Experience in Design Control; including, Design change, Process change, verification and Validation and risk management.
  • Good understanding of CFDA, ISO and FDA regulations.
  • Demonstrate ability to analyze problems in a structured and systematic manner with the proven ability to interpret data and to troubleshoot and resolve technical issues.
  • Excellent quantitative skills and knowledge of statistics enabling the ability to work cross-functionally with statisticians.
  • Ability to multi-task and to support multiple project teams in cross functional settings.
  • Excellent organizational, oral and written communication skills.
  • Ability to write clear and concise Plans and reports and other quality documents.
Position Requirements
  • BS in chemistry, biology or biological sciences, with 6-10 yrs industry experience, or MA/MS with 3-6 yrs industry experience
  • Previous IVDD  experience  in a technical role
  • Previous Management experience

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